Last synced on 14 November 2025 at 11:06 pm

InTRAkit

Page Type
Cleared 510(K)
510(k) Number
K162097
510(k) Type
Traditional
Applicant
Medtronic Vascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2016
Days to Decision
111 days
Submission Type
Summary

InTRAkit

Page Type
Cleared 510(K)
510(k) Number
K162097
510(k) Type
Traditional
Applicant
Medtronic Vascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2016
Days to Decision
111 days
Submission Type
Summary